Document Quality Control Associate

A Document Quality Control Associate job is available in Memphis, TN through Adecco Medical and Science.

Key Responsibilities:

Complete Quality Control documentation for production and distribution in accordance with organizational procedures, SOPs, current Good Tissue Practices, FDA and other regulatory requirements.
Lead by example and enforce Good Documentation Practices within operations.
Support Quality activities in production and distribution for equipment qualification, including calibration and preventive maintenance activities.
Support documentation and processes in compliance with the Quality System.
Uphold regulatory guidelines set forth by the FDA, AATB, HHS, and OSHA.

Education & Qualification:

Bachelor’s of Science, engineering, or related technical field preferred.
2+ years of experience working within an FDA regulated industry (e.g., Medical Device, Pharmaceutical, HCT/P).
Knowledge of 21 CFR 820 and/or 1271, ISO 13485, AATB Standards, and ISO 14971 preferred.
MUST be able to work 2nd shift (3:00pm -11:00pm)

If you are interested in the Document Quality Control Associate job, please click APPLY NOW. #LI-MH1

Equal Opportunity Employer Veterans/Women/Disabled/Minorities

  • Apply with Adecco

Reference number US_EN_2_106405_332284